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Journal Abstract Search
369 related items for PubMed ID: 7088015
1. Variability in nerve biopsy findings in a kinship with dominantly inherited Charcot-Marie-Tooth disease. Van Weerden TW, Houthoff HJ, Sie O, Minderhoud JM. Muscle Nerve; 1982 Mar; 5(3):185-96. PubMed ID: 7088015 [No Abstract] [Full Text] [Related]
2. [Three cases of Charcot-Marie-Tooth disease with neural deafness-the classification and sural nerve pathology (author's transl)]. Kim I, Ohnishi A, Kuroiwa Y. Rinsho Shinkeigaku; 1980 Apr; 20(4):264-70. PubMed ID: 7408330 [No Abstract] [Full Text] [Related]
3. Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography. Buchthal F, Behse F. Brain; 1977 Mar; 100 Pt 1():41-66. PubMed ID: 861715 [No Abstract] [Full Text] [Related]
4. [Charcot-Marie-Tooth neural muscular atrophy (HMSN type I) with isolated tumerous hypertrophy of the median nerve]. Berger W, Goth D, Ketelsen U. Nervenarzt; 1982 Dec; 53(12):725-8. PubMed ID: 7155235 [No Abstract] [Full Text] [Related]
8. [Four cases of hereditary motor and sensory neuropathy in childhood--light and electron microscopic studies of sural nerve biopsies]. Sugie Y, Sugama M, Sugama S, Kosaka S, Shibuya T, Sugie H, Fukuyama Y. No To Hattatsu; 1985 Nov; 17(6):500-6. PubMed ID: 4084416 [No Abstract] [Full Text] [Related]
9. Electrophysiological and sural nerve biopsy studies in patients with Freidreich's ataxia and Charcot-Marie-Tooth disease. McLeod JG. Proc Aust Assoc Neurol; 1970 Nov; 7():89-95. PubMed ID: 5514829 [No Abstract] [Full Text] [Related]
10. Nemaline rod myopathy and Charcot-Marie-Tooth disease. Report of a case in a 10-year-old girl. Danon MJ, Sarpel G, Manaligod JR. Arch Neurol; 1980 Feb; 37(2):123-7. PubMed ID: 7356407 [Abstract] [Full Text] [Related]
11. Hypertrophic Charcot-Marie-Tooth disease. Light and electron microscope studies of the sural nerve. Low PA, McLeod JG, Prineas JW. J Neurol Sci; 1978 Jan; 35(1):93-115. PubMed ID: 624962 [Abstract] [Full Text] [Related]
12. Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 gene. Kabzińska D, Kochański A, Drac H, Ryniewicz B, Rowińska-Marcińska K, Hausmanowa-Petrusewicz I. Neuropediatrics; 2005 Jun; 36(3):206-9. PubMed ID: 15944907 [Abstract] [Full Text] [Related]
13. [Formation of "onion bulbs" in Charcot-Marie-Tooth and Dejerine-Sottas hypertrophic neuropathies]. Jedrzejowska H, Drac H, Sawicka E. Neuropatol Pol; 1975 Jun; 13(1):93-106. PubMed ID: 1118064 [No Abstract] [Full Text] [Related]